Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing Recalled by Johnson Matthey Inc. Due to Failed Impurities/Degradation Specifications: Unknown impurity above specification limits.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Johnson Matthey Inc. directly.
Affected Products
Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing, processing or repackaging, 416.95 g glass container, Rx ONLY, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742.
Quantity: 416.95 g glass container
Why Was This Recalled?
Failed Impurities/Degradation Specifications: Unknown impurity above specification limits.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Johnson Matthey Inc.
Johnson Matthey Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report